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Fig. 6 | Journal of Translational Medicine

Fig. 6

From: Anthocyanin improves kidney function in diabetic kidney disease by regulating amino acid metabolism

Fig. 6

GSVA analysis of KEGG pathways for ANT trend metabolites and metabolic pathways altered by ANT in the kidney and serum. The enrichment score for nine KEGG pathways by GSVA analysis in the kidney (A) and serum (C) among the CT, DKD, and ANT three groups. The red and blue nodes represent enrichment score of KEGG pathways in each sample for three groups, respectively. The gray and purple nodes represent P value of KEGG pathways (moderated t-test, P < 0.05). The differentially activated KEGG pathways between the DKD vs. CT and ANT vs. DKD groups in the kidney (B) and serum (D). The blue and orange bands represent the activated KEGG pathways of the DKD vs. CT and ANT vs. DKD groups, respectively, and the gray bands represent the nonactivated KEGG pathways. (E) The diagram of a part of the taurine and hypotaurine metabolism pathway. The expression of taurine, 5-L-glutamyl-taurine, and acetyl-CoA is shown in (E). The enzymatic expression of Ado, Cdo1, Fmo5, and Ggt1 is shown in (E). Other metabolites, including hypotaurine, cysteamine, L-cysteine, and 3-sulfino-L-alanine, were not identified in the current study. (F) The diagram of a part of the tryptophan and tyrosine metabolism pathway. The expression of L-tryptophan, L-kynurenine, 5-methoxyindoleacetate, indoleacetaldehyde, maleic acid, fumaric acid, and indole-5,6-quinone is shown in (F). The expression of Aldh1a7, Acat1, Cat, Hgd, Comt, and Fah is shown in (F). Other metabolites, including 3-hydroxyanthranilate, cinnavalininate, Acetyl-CoA, tyrosine, L-DOPA, L-metanephrine, and 4-maleylacetoacetate, were not identified in the current study

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